Relaxant effects of butylidenephthalide in isolated dog blood vessels

Wun Chang Ko, Chao Chiun Liao, Chih Hsien Shih, Chien Bang Lei, Chi Ming Chen

研究成果: 雜誌貢獻文章同行評審

30 引文 斯高帕斯(Scopus)

摘要

We investigated the reason why butylidenephthalide (Bdph) can have an antianginal effect without changing blood pressure in conscious rats. Isolated dog coronary artery (CA), femoral vein (FV), femoral artery (FA), and mesenteric artery (MA) were used to evaluate the relaxant effects of Bdph. Bdph concentration-dependently relaxed isolated CA, FV, FA, and MA precontracted by KCl (60 mM) and phenylephrine (phe, 5 μM) with the exception that CA was precontracted by prostaglandin F2a (PGF2a, 2μM) instead of phe. The potency order of Bdph to these blood vessels was FV > CA > FA ≥ MA. Bdph also concentration-dependently and non-competitively inhibited cumulative KCl (5-120 mM)- and phe (0.1 - 100 μM)-induced contractions in normal, and inhibited cumulative Ca2+-induced contractions in depolarized blood vessels. The potency order of Bdph to these blood vessels was FV > CA > FA ≥ MA. Bdph (0.02-0.04 mM) concentration-dependently and leftward-shifted the log concentration-response curves in parallel and significantly increased the pD2 value of forskolin, but not nitroprusside in FV. Bdph (0.1 mM) did both in CA. Bdph (0.225-0.45 mM) did the opposite to that of nitroprusside, but not forskolin, in FA. Bdph (0.45-0.9 mM) did neither in MA. Bdph (0.1-1 mM) significantly inhibited cAMP-but not cGMP-PDE activities in these four blood vessels, suggesting that Bdph more selectively inhibited the former in these tissues. The above results suggest that the higher potencies of Bdph on FV and CA than on FA and MA, may be interpreted as the reason why Bdph is useful in the treatment of angina pectoris without changing blood pressure, after Bdph administration in vivo, because the venoreturn may be reduced and the coronary flow may be increased without affecting the arterioles, such as MA, the main determinant of blood pressure.
原文英語
頁(從 - 到)1004-1009
頁數6
期刊Planta Medica
68
發行號11
DOIs
出版狀態已發佈 - 十一月 1 2002

ASJC Scopus subject areas

  • 植物科學
  • 有機化學
  • 藥物發現
  • 藥理

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